Rabbit Polyclonal Antibody to SLC26A4
货号：
P12415
别名：
EVA; PDS; DFNB4; TDH2B
应用：
IHC
反应种属：
Human, Mouse, Rat
抗体类型：
Primary antibody
Swissprot：
O43511
规格：
目录价
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Description |
|---|
Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters. |
Specification |
|
|---|---|
| Aliases | EVA; PDS; DFNB4; TDH2B |
| Swissprot | O43511 |
| Host/Isotype | Rabbit IgG |
| Antibody Type | Primary antibody |
| Storage | Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles. |
| Species Reactivity | Human, Mouse, Rat |
| Immunogen | Synthetic peptide of human SLC26A4 |
| Formulation | Purified antibody in PBS with 0.05% sodium azide and 50% glycerol. |
Application |
|
|---|---|
| IHC | 1/50-1/200 |
| ELISA | 1/5000-1/10000 |
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